Clonazepam
- Product NDC
- 0781-5567
- 11-digit product format
- 007815567
- Labeler code
- 0781
- Product ID
- 0781-5567_4d8fee88-4d24-4975-b0de-a2e9ae2014fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA074979
- Marketing category
- ANDA
- Marketing start
- 2016-07-01
- Marketing end
- 2021-11-30
- Substance
- CLONAZEPAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-5567-01 | 00781556701 | 100 TABLET in 1 BOTTLE (0781-5567-01) | 100 tablet | 2017-06-27 | 2021-11-30 | No | No | Current |
| 0781-5567-05 | 00781556705 | 500 TABLET in 1 BOTTLE (0781-5567-05) | 500 tablet | 2017-06-26 | 2021-10-31 | No | No | Current |
| 0781-5567-10 | 00781556710 | 1000 TABLET in 1 BOTTLE (0781-5567-10) | 1000 tablet | 2017-06-27 | 2021-11-30 | No | No | Current |